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Body Mass Index at the Time of Diagnosis of Autoimmune Type 1 Diabetes in Children - 25/03/13

Doi : 10.1016/j.jpeds.2012.09.017 
Brett M. Kaminski, MPH 1, Georgeanna J. Klingensmith, MD 2, Roy W. Beck, MD, PhD 1, , William V. Tamborlane, MD 3, Joyce Lee, MD 4, Krishna Hassan, MD 5, Desmond Schatz, MD 6, Craig Kollman, PhD 1, Maria J. Redondo, MD, PhD 5

Pediatric Diabetes Consortium

  A list of members of the Pediatric Diabetes Consortium is available at www.jpeds.com (Appendix).

1 Jaeb Center for Health Research, Tampa, FL 
2 Department of Pediatrics, Barbara Davis Center for Childhood Diabetes, University of Colorado School of Medicine, Aurora, CO 
3 Department of Pediatric Endocrinology, Yale University, New Haven, CT 
4 Department of Pediatric Endocrinology, Mott Children’s Hospital, University of Michigan, Ann Arbor, MI 
5 Department of Pediatrics, Texas Children’s Hospital, Baylor College of Medicine, Houston, TX 
6 Department of Pediatrics, University of Florida, Gainesville, FL 

Reprint requests: Roy W. Beck, MD, PhD, Jaeb Center for Health Research, 15310 Amberly Drive, Suite 350 Tampa, FL.

Abstract

Objectives

To describe the body mass index (BMI) distribution of children developing autoimmune type 1 diabetes (T1D) compared with the general population and to assess factors associated with BMI at T1D onset.

Study design

Children age 2-<19 years enrolled in the Pediatric Diabetes Consortium at 7 US pediatric diabetes centers at T1D onset were included. Eligibility for analysis required a diagnosis of T1D, ≥1 positive diabetes autoantibody, and availability of BMI within 14 days of diagnosis. BMI at diagnosis was compared with the general population as described by the 2000 Centers for Disease Control. Regression analysis was used to assess the association between BMI and various participant characteristics.

Results

BMI scores for the 490 participants were slightly lower than the 2000 Centers for Disease Control population (P = .04). The median BMI percentile for age and sex was 48th, 11% of the children were overweight (BMI ≥85th and <95th percentile), 8% obese (BMI ≥95th and <99th percentile), and 2% severely obese (≥99th percentile), percentages that were comparable across age and sex groups. Higher BMI Z-scores were associated with African American and Hispanic race/ethnicity (P = .001) and lower hemoglobin A1c (P < .001), and diabetic ketoacidosis, age, and Tanner stage were not associated.

Conclusions

Although the BMI distribution in children developing autoimmune T1D was lower than that of the general population, 21% of children were obese or overweight. Youth who are overweight, obese, racial/ethnic minority, and/or present without diabetic ketoacidosis should not be presumed to have type 2 diabetes because many patients with autoantibody-positive T1D present with the same clinical characteristics.

Le texte complet de cet article est disponible en PDF.

Keyword : BMI, CDC, DKA, HbA1c, NHANES, PDC, T1D, T2D


Plan


 The Pediatric Diabetes Consortium and its activities are supported by the Jaeb Center for Health Research Foundation through an unrestrictive grant from Novo Nordisk, Inc. The University of Michigan center was supported by the Michigan Diabetes Research and Training Center funded by the National Institute of Diabetes and Digestive and Kidney Diseases (DK020572). Novo Nordisk and NIDDK were not involved in: (1) study design; (2) the collection, analysis, and interpretation of data; (3) the writing of the report; and (4) the decision to submit the manuscript for publication. The authors declare no conflicts of interest.


© 2013  Mosby, Inc. Tous droits réservés.
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Vol 162 - N° 4

P. 736 - avril 2013 Retour au numéro
Article précédent Article précédent
  • Social Determinants of Health on Glycemic Control in Pediatric Type 1 Diabetes
  • Caroline S. Zuijdwijk, Meaghan Cuerden, Farid H. Mahmud
| Article suivant Article suivant
  • Impact of Gestational Diabetes Mellitus on Pubertal Changes in Adiposity and Metabolic Profiles in Latino Offspring
  • Jaimie N. Davis, Erica P. Gunderson, Lauren E. Gyllenhammer, Michael I. Goran

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